510(k) K073144 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LANX INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Lanx, LLC, Broomfield CO, US |
| Decision | Substantially Equivalent, Jan 24, 2008 |
| Received | Nov 7, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073144
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.